摘要
Bruton酪氨酸激酶(Bruton tyrosine kinase,BTK)是B细胞受体(B cell receptor,BCR)信号通路的重要中介分子,在B细胞淋巴瘤的形成中发挥重要作用。伊布替尼(Ibrutinib)是口服不可逆BTK抑制剂,可有效抑制B细胞增殖并诱导其凋亡。
Bruton’s tyrosine kinase(BTK),an important mediator of the BCR signal pathway,plays an important role in the formation of B-cell lymphoma.Ibrutinib is an oral active BTK inhibitor that effectively inhibits the malignant proliferation and induces apoptosis of B cells.As a single agent,it has shown extremely promising activity in relapsed and refractory B-cell lymphoma patients with well tolerability and acceptable toxicities.In our department,3 patients with relapsed and refractory B-cell lymphoma received single-agent Ibrutinib achieved remission in short time.
出处
《临床血液学杂志》
CAS
2020年第5期644-646,共3页
Journal of Clinical Hematology
基金
国家自然科学基金(No:81700177)。
关键词
伊布替尼
BTK抑制剂
B细胞淋巴瘤
Ibrutinib
Bruton tyrosine kinase inhibitor
B cell lymphoma